Topotecan Weekly Versus Topotecan Day 1-5 in Patient With Platin-resistant Ovarian Cancer
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 194
- 试验地点
- 1
- 主要终点
- Rate of CR and PR in each arm
研究概览
简要总结
Comparison of topotecan weekly vs. topotecan day 1-5. The compatibility and activity are to be examined.
详细描述
Topotecan belongs to the most effective medicaments in the therapy of relapsed platin-resistant ovarian cancer. Due to the low rate of hematological toxicities of grade 3 or 4 weekly application may be an improvement of therapy. None randomised study exists comparing a weekly topotecan application with an application on day 1-5. This study will compare the two applications in regard to: rate of complete or partial remissions, rate of toxicity, quality of life, progression free survival, overall survival.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •patients with histologically-confirmed ovarian cancer
- •relapse within 6 month after primary therapy
- •primary therapy with platin and taxan
- •>= 18 years
- •leukocytes >= 3.000/ µl
- •platelet >= 100.000/ µl
- •neutrophil >= 1.500/ µl
- •written informed consent
排除标准
- •earlier topotecan therapy
- •simultaneous or planned radiotherapy
- •secondary malignancy
研究组 & 干预措施
A
干预措施: Topotecan (Drug)
B
干预措施: Topotecan (Drug)
结局指标
主要结局
Rate of CR and PR in each arm
时间窗: every 12 weeks
次要结局
- Toxicity of topotecan treatment(after each cycle)
- Progression-free survival of both arms(every 12 weeks)
